Abstract
Triazinane diones, readily generated by a recently reported multicomponent reaction, can be easily alkylated with various alkyl halides, allowing a wide variety of complexity-generating secondary reactions. Because of the high variability of the initial multicomponent reactions and the multiple possibilities for participation of substituents in the secondary reactions, a highly diverse set of complex products was obtained in short and efficient reaction sequences. © 2008 The Royal Society of Chemistry.
| Original language | English |
|---|---|
| Pages (from-to) | 3158-65 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 6 |
| Issue number | 17 |
| DOIs | |
| Publication status | Published - 2008 |
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Dive into the research topics of 'Generation of molecular diversity using a complexity-generating MCR-platform towards triazinane diones'. Together they form a unique fingerprint.Datasets
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CCDC 686384: Experimental Crystal Structure Determination
Groenendaal, B. (Contributor), Ruijter, E. (Contributor), De Kanter, F. J. J. (Contributor), Lutz, M. (Contributor), Spek, A. L. (Contributor) & Orru, R. V. A. (Contributor), Unknown Publisher, 1 Jan 2009
DOI: 10.5517/ccr17ff, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccr17ff&sid=DataCite
Dataset / Software: Dataset